Comparison of contractile behavior of native murine ventricular tissue and cardiomyocytes derived from embryonic or induced pluripotent stem cells

Jiaoya Xi, Markus Khalil, Nava Shishechian, Tobias Hannes, Kurt Pfannkuche, Huamin Liang, Azra Fatima, Moritz Haustein, Frank Suhr, Wilhelm Bloch, Michael Reppel, Tomo Sarić, Marius Wernig, Rudolf Jänisch, Konrad Brockmeier, Jürgen Hescheler, Frank Pillekamp

Publikation: Beitrag in FachzeitschriftZeitschriftenaufsätzeForschung

27 Quellenangaben (Web of Science)

Abstract

Cardiomyocytes generated from embryonic stem cells (ESCs) and induced pluripotent stem (iPS) cells are suggested for repopulation of destroyed myocardium. Because contractile properties are crucial for functional regeneration, we compared cardiomyocytes differentiated from ES cells (ESC-CMs) and iPS cells (iPS-CMs). Native myocardium served as control. Murine ESCs or iPS cells were differentiated 11 d in vitro and cocultured 5-7 d with irreversibly injured myocardial tissue slices. Vital embryonic ventricular tissue slices of similar age served for comparison. Force-frequency relationship (FFR), effects of Ca(2+), Ni(2+), nifedipine, ryanodine, beta-adrenergic, and muscarinic modulation were studied during loaded contractions. FFR was negative for ESC-CMs and iPS-CMs. FFR was positive for embryonic tissue and turned negative after treatment with ryanodine. In all groups, force of contraction and relaxation time increased with the concentration of Ca(2+) and decreased with nifedipine. Force was reduced by Ni(2+). Isoproterenol (1 microM) increased the force most pronounced in embryonic tissue (207+/-31%, n=7; ESC-CMs: 123+/-5%, n=4; iPS-CMs: 120+/-4%, n=8). EC(50) values were similar. Contractile properties of iPS-CMs and ESC-CMs were similar, but they were significantly different from ventricular tissue of comparable age. The results indicate immaturity of the sarcoplasmic reticulum and the beta-adrenergic response of iPS-CMs and ESC-CMs.

OriginalspracheEnglisch
ZeitschriftFASEB journal : official publication of the Federation of American Societies for Experimental Biology
Jahrgang24
Ausgabenummer8
Seiten (von - bis)2739-2751
Seitenumfang13
DOIs
PublikationsstatusVeröffentlicht - 01.08.2010

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